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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM1018194"><item key="CELL TYPE">IL10+CD25+CD4+ T-cells</item></item></item><item><item key="GSM1018194"><item key="CELL TYPE">IL10+CD25+CD4+ T-cells</item></item></item><item><item key="GSM1018196"><item key="CELL TYPE">IL10-CD25+CD4+ T-cells</item></item></item><item><item key="GSM1018196"><item key="CELL TYPE">IL10-CD25+CD4+ T-cells</item></item></item></item><item key="id">7045</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">The ability of Treg-cells to produce interleukin-10 (IL-10) is important for the limitation of  inflammation at environmental interfaces...</item><item key="geo_gse_id">E-GEOD-41492</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">4</item><item key="tags"><item>colon</item><item>interleukin</item><item>interleukin-10</item><item>lung</item><item>lymph</item><item>lymph node</item><item>surface</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-41492_A-AFFY-45</item><item key="slug">sequential-induction-of-effector-function-tissue-m</item><item key="geo_gds_id"/><item key="name">Sequential induction of effector function, tissue migration and cell death during polyclonal activation of regulatory T-cells</item><item key="created">Nov.12, 2014</item><item key="summary">The ability of Treg-cells to produce interleukin-10 (IL-10) is important for the limitation of  inflammation at environmental interfaces like colon or lung. Under steady state conditions, however,  only few Treg-cells produce IL-10 ex vivo. To investigate the origin and fate of IL-10 producing Tregcells  we used a superagonistic mouse anti-mouse CD28 mAb (CD28SA) for polyclonal in vivo  stimulation of Treg-cells, which not only led to numeric expansion but also to a dramatic increase in IL-  10 production. IL-10 secreting Treg-cells strongly upregulated surface receptors associated with  suppressive function, and had higher but IL-10 independent, in vitro suppressive capacity than nonproducing  Treg-cells. Furthermore, polyclonally expanding Treg-cells shifted their migration receptor  pattern after activation from a lymph node-seeking to an inflammation-seeking phenotype, explaining  the preferential recruitment of IL-10 producers to sites of ongoing immune responses. Finally, we  observed that IL-10 producing Treg-cells from CD28SA stimulated mice were more apoptosis-prone in  vitro than their IL-10 negative counterparts. These findings support a model where prolonged activation  of Treg-cells results in terminal differentiation towards an IL-10 producing effector phenotype  associated with a limited lifespan, implicating built-in termination of immunosuppression. total samples analysed are 4</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-41492</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-41492/samples/</item></data></biogps>
